Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team.
Responsibilities:
Conduct site monitoring visits (initiation, routine, close-out) in line with SOPs, ICH-GCP, and study requirements
Ensure patient safety and protocol compliance, including informed consent and eligibility verification
Perform source data verification, resolve queries, and maintain high data quality and integrity
Maintain site documentation (ISF/eTMF) and ensure audit readiness at all times
Manage investigational product accountability and site supplies in line with protocol requirements
Collaborate with study teams to deliver milestones, prepare reports, and support timelines
Requirements:
Degree in Life Sciences, Nursing, or related field (or equivalent experience)
Minimum 2 years of independent clinical monitoring experience
Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements
Ability to work independently, with good organisation and problem-solving skills
Experience with eClinical systems (e.g. CTMS, eCRF) and solid MS Office skills
Fluency in English and Romanian languages; willingness to travel (~60%)
Learn more about our EEO & Accommodations request here.